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(R)-(+)-2-Methyl-2-propanesulfinamide_Molecular_structure_CAS_196929-78-9)
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(R)-(+)-2-Methyl-2-propanesulfinamide

Catalog No. 497401 Name Sigma Aldrich
CAS Number 196929-78-9 Website http://www.sigmaaldrich.com
M. F. C4H11NOS Telephone 1-800-521-8956
M. W. 121.20124 Fax
Purity 98% Email
Storage Chembase ID: 67396

SYNONYMS

Title
(R)-(+)-2-甲基-2-丙烷亚磺酰胺
IUPAC name
(R)-2-methylpropane-2-sulfinamide
IUPAC Traditional name
(R)-2-methylpropane-2-sulfinamide

DATABASE IDS

MDL Number MFCD05861479
CAS Number 196929-78-9
PubChem SID 24873117

PROPERTIES

Linear Formula (CH3)3CS(O)NH2
Purity 98%
Melting Point 103-107 °C(lit.)
Optical Rotation [α]20/D +4°, c = 1.0242 in chloroform stab. with amylenes
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Application
Can be readily transformed into P,N-sulfinyl imine ligands through condensation with aldehydes and ketones, which can undergo iridium-catalyzed asymmetric hydrogenation of olefins.1
Preparation of β-chloro sulfinamides in a synthesis of chiral azridines. Also used to prepare an organocatalyst for enantioselective reduction of imines.
Useful reagent for synthesizing chiral amines.
Ellman′s Sulfinamides
Packaging
1, 5 g in glass bottle
25 g in poly bottle
Description (简体中文)
Application
合成手性胺的有效试剂。
在手性氮丙啶的合成中制备 β-氯代亚磺酰胺。也可用于制备亚胺对映选择性还原反应的有机催化剂。
易与醛和酮发生缩合反应,转化为 P,N-亚磺酰亚胺配体,该配体可参与烯烃的铱催化不对称氢化反应。1
Ellman′s Sulfinamides
包装
1, 5 g in glass bottle
25 g in poly bottle

REFERENCES